Description
Our client, a global pharmaceutical company, are looking for an experienced Qualification Engineer to support them on the implementation of a new pellet production line at their site in Northern Germany.Location: 30 mins from Hannover, Germany
Duration: 6 – 12 months – extensions are possible
Tasks:
- Creating qualification documents, carry out risk analysis.
- Supervision of technical changes on equipment, auxiliary equipment and facilities.
- Implementation of DQ / IQ / OQ (plans / test protocols / reports, reviews).
- Implementation of all planned activities within the project.
- Preparation of qualification documents for templates (qualification plan, risk analysis, qualification report, Test Protocols, Reviews, etc.).
- Support of the project engineers for specifications.
- Supervision and coordination of 3rd party suppliers.
- Technical and professional review of technical documents.
Requirements:
- Degree in process engineering, chemistry, Pharmacy or biotechnology.
- Several years of professional experience in the field of qualification of GxP, relevant equipment / systems.
- CSV experience desirable.
- Project work: knowledge of MS Office.
- Languages: German and English fluent spoken and written.